Canonical Allele Identifier: CA2320767888

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125242G= , CM000681.2:g.7125242G=	GRCh38
NC_000019.9:g.7125253G= , CM000681.1:g.7125253G=	GRCh37
NC_000019.8:g.7076253G=	NCBI36
NG_008852.2:g.173759C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3258+41C= MANE Select	ENSP00000303830.4:n.3258+41C=
ENST00000302850.9:c.3258+41C=	ENSP00000303830.4:n.3258+41C=
ENST00000341500.9:c.3222+41C=	ENSP00000342838.4:n.3222+41C=
ENST00000593970.1:n.104+41C=
NM_000208.2:c.3258+41C=	NP_000199.2:n.3258+41C=
NM_000208.3:c.3258+41C=	NP_000199.2:n.3258+41C=
NM_001079817.1:c.3222+41C=	NP_001073285.1:n.3222+41C=
NM_001079817.2:c.3222+41C=	NP_001073285.1:n.3222+41C=
XM_011527988.1:c.3333+41C=	XP_011526290.1:n.3333+41C=
XM_011527989.1:c.3297+41C=	XP_011526291.1:n.3297+41C=
XM_011527988.2:c.3255+41C=	XP_011526290.2:n.3255+41C=
XM_011527989.3:c.3219+41C=	XP_011526291.2:n.3219+41C=
NM_000208.4:c.3258+41C= MANE Select	NP_000199.2:n.3258+41C=
NM_001079817.3:c.3222+41C=	NP_001073285.1:n.3222+41C=